Term Name:	autosomal dominant cerebellar ataxia, deafness and narcolepsy
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by ataxia, sensorineal deafness, narcolepsy with cataplexy, and dementia, has_material_basis_in mutation in the DNMT1 gene.
Ontology:	Human Disease [DOID:0050968]   ( DOID:0050968 )